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• Abametapir (Catalog# : 161227111, Cas# : 1762-34-1)Abametapir is the active ingredient of Xeglyze Lotion. Abametapir inhibits metallopro
• Alantolactone (Catalog# : 161227107, Cas# : 546-43-0)Alantolactone, a naturally occurring eudesmane-type sesquiterpene lactone (SL), could
• AS101 (Catalog# : 161227106, Cas# : 106566-58-9)AS101, a potent in vitro and in vivo immunomodulator, is a novel inhibitor of IL-1bet
• ACP-196 (Catalog# : 16122783, Cas# : 1420477-60-6)Acalabrutinib is a selective second-generation Brutons tyrosine kinase (BTK) inhibito
• APS-2-79 (Catalog# : 16122775, Cas# : 2002381-31-7)APS-2-79 is a MAPK antagonist that modulating KSR-dependent MAPK signalling by antago
• Aprotinin (Catalog# : 16122761, Cas# : 9087-70-1)Aprotinin is a small protein serine protease inhibitor, used to reduce perioperative
• A-366 (Catalog# : 16122743, Cas# : 1527503-11-2)A-366 is a potent and selective G9a/GLP histone lysine methyltransferase inhibitor wi
• AZD0156 (Catalog# : 16122713, Cas# : 1821428-35-6)AZD0156 is a potent and selective inhibitors of ATM kinase, with potential chemo-/rad
• APTSTAT3-9R (Catalog# : 16122704)APTSTAT3-9R is a specific STAT3-binding peptide with addition of a cell-penetrating m
• AGN 205728 (Catalog# : 6111520, Cas# : 859498-05-8)AGN 205728 is a potent and selective RAR antagonist with Ki/IC95 values of 3 nM/ 0.6
• AGN 205327 (Catalog# : 6111519)AGN 205327 is a potent synthetic RARs agonist with EC50 of 3766/734/32 nM for RAR// r
• AGN 195183 (Catalog# : 6111517, Cas# : 367273-07-2)AGN 195183 is a potent and selective agonist of RAR(Kd=3 nM) with improved binding se
• AGN 194310 (Catalog# : 6111516, Cas# : 229961-45-9)AGN 194310(VTP-194310) is a potent and selective pan-RARs agonist with Kd values of 3
• Acetazolamide D3 (Catalog# : 6111513, Cas# : 1189904-01-5)Acetazolamide D3 is deuterium labeled Acetazolamide, which is a potent carbonic anhyd
• APS-2-79 (Catalog# : 6111501, Cas# : 2002381-25-9)APS-2-79 is an antagonist of MEK phosphorylation by RAF through direct binding of the
• (+)-Apogossypol (Catalog# : 61125, Cas# : 66389-74-0)(+)-Apogossypol(Apogossypol; NSC736630) is a potent inhibitor of Bcl-2 family protein
• A-836339 (Catalog# : 6111107, Cas# : 959746-77-1)A-836339 is a cannabinoid CB2 receptor-selective agonist; exhibits high potencies at
• AB-MECA (Catalog# : 6111105, Cas# : 152918-26-8)AB-MECA is a high affinity A3 adenosine receptor agonist, has high affinity for recom
• Amitifadine hydrochloride (Catalog# : 6111104, Cas# : 410074-74-7)Amitifadine hydrochloride is a triple reuptake inhibitor (TRI) or serotonin-norepinep
• ATI-2341 (Catalog# : 6111101, Cas# : 1337878-62-2)ATI-2341, pepducin targeting the C-X-C chemokine receptor type 4 (CXCR4), is an allos
• Auristatin F (Catalog# : 6111022, Cas# : 163768-50-1)Auristatin F is a cytotoxic tubulin modifier with potent and selective antitumor acti
• Auristatin E (Catalog# : 6111021, Cas# : 160800-57-7)Auristatin E is a cytotoxic tubulin modifier with potent and selective antitumor acti
• ABT-639 (Catalog# : 6111011, Cas# : 1235560-28-7)ABT-639 is a novel, peripherally acting, selective T-type Ca2+ channel blocker. ABT-6
• 3-aMino-1-Methyl-1H-pyrazole-4-carbonitrile (Catalog# : 6111001, Cas# : 21230-50-2)3-aMino-1-Methyl-1H-pyrazole-4-carbonitrile 21230-50-2
• 360A (Catalog# : 611935, Cas# : 794458-56-3)360A is a strong affinity and selectivity inhibitor of G-quadruplex structures.
• AT7519 trifluoroacetate (Catalog# : 611916, Cas# : 1431697-85-6)AT7519 trifluoroacetate is a multi-CDK inhibitor for CDK1, 2, 4, 6 and 9 with IC50 of
• Ampkinone (Catalog# : 611810, Cas# : 1233082-79-5)Ampkinone is a small molecule activator of AMPK; stimulate functional activation of A
• AT7867 dihydrochloride (Catalog# : 611806, Cas# : 1431697-86-7)AT7867 Hcl is a potent ATP-competitive inhibitor of Akt1/2/3 and p70S6K/PKA with IC50
• ARQ-092 (Catalog# : 611805, Cas# : 1313881-70-7)ARQ-092 is an Akt inhibitor extracted from patent US/20150299195A1, compound A.
• Akt1 and Akt2-IN-1 (Catalog# : 611804, Cas# : 893422-47-4)Akt1 and Akt2-IN-1 is an allosteric inhibitor of Akt1 (IC50 = 3.5 nM) and Akt2 (IC50